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Thiasporines A–C, Thiazine and Thiazole Derivatives from a Marine-Derived Actinomycetospora chlora
[Image: see text] Thiasporine A (1), the first natural product with a 5-hydroxy-4H-1,3-thiazin-4-one moiety, along with two new thiazole derivatives, thiasporines B and C (2 and 3), were isolated from the marine-derived Actinomycetospora chlora SNC-032. The structures of 1–3 were established on the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society and American Society of Pharmacognosy
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380196/ https://www.ncbi.nlm.nih.gov/pubmed/25584783 http://dx.doi.org/10.1021/np500929z |
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author | Fu, Peng MacMillan, John B. |
author_facet | Fu, Peng MacMillan, John B. |
author_sort | Fu, Peng |
collection | PubMed |
description | [Image: see text] Thiasporine A (1), the first natural product with a 5-hydroxy-4H-1,3-thiazin-4-one moiety, along with two new thiazole derivatives, thiasporines B and C (2 and 3), were isolated from the marine-derived Actinomycetospora chlora SNC-032. The structures of 1–3 were established on the basis of comprehensive spectroscopic analysis and chemical methods. Thiasporine A showed cytotoxicity against the non-small-cell lung cancer cell line H2122 with an IC(50) value of 5.4 μM. |
format | Online Article Text |
id | pubmed-4380196 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Chemical
Society and American Society of Pharmacognosy |
record_format | MEDLINE/PubMed |
spelling | pubmed-43801962016-01-13 Thiasporines A–C, Thiazine and Thiazole Derivatives from a Marine-Derived Actinomycetospora chlora Fu, Peng MacMillan, John B. J Nat Prod [Image: see text] Thiasporine A (1), the first natural product with a 5-hydroxy-4H-1,3-thiazin-4-one moiety, along with two new thiazole derivatives, thiasporines B and C (2 and 3), were isolated from the marine-derived Actinomycetospora chlora SNC-032. The structures of 1–3 were established on the basis of comprehensive spectroscopic analysis and chemical methods. Thiasporine A showed cytotoxicity against the non-small-cell lung cancer cell line H2122 with an IC(50) value of 5.4 μM. American Chemical Society and American Society of Pharmacognosy 2015-01-13 2015-03-27 /pmc/articles/PMC4380196/ /pubmed/25584783 http://dx.doi.org/10.1021/np500929z Text en Copyright © 2015 American Chemical Society and American Society of Pharmacognosy This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Fu, Peng MacMillan, John B. Thiasporines A–C, Thiazine and Thiazole Derivatives from a Marine-Derived Actinomycetospora chlora |
title | Thiasporines A–C, Thiazine and Thiazole Derivatives
from a Marine-Derived Actinomycetospora chlora |
title_full | Thiasporines A–C, Thiazine and Thiazole Derivatives
from a Marine-Derived Actinomycetospora chlora |
title_fullStr | Thiasporines A–C, Thiazine and Thiazole Derivatives
from a Marine-Derived Actinomycetospora chlora |
title_full_unstemmed | Thiasporines A–C, Thiazine and Thiazole Derivatives
from a Marine-Derived Actinomycetospora chlora |
title_short | Thiasporines A–C, Thiazine and Thiazole Derivatives
from a Marine-Derived Actinomycetospora chlora |
title_sort | thiasporines a–c, thiazine and thiazole derivatives
from a marine-derived actinomycetospora chlora |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380196/ https://www.ncbi.nlm.nih.gov/pubmed/25584783 http://dx.doi.org/10.1021/np500929z |
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